Azelaic Acid → Bis(2-hydroxyethyl) azelate

HRID 328313

Reaktionsgleichung

Reaktionsgleichung von HRID 328313
[C:1]([OH:13])(=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9]([OH:11])=[O:10].[CH2:14]1[O:16][CH2:15]1.[CH2:17]([C:21](C)=[O:22])C(C)C>>[OH:22][CH2:21][CH2:17][O:10][C:9](=[O:11])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:1]([O:13][CH2:15][CH2:14][OH:16])=[O:12]

Komponenten

4

Edukt 3

HCID 2266Azelaic AcidHCID 6354Ethylene OxideHCID 7909Methyl Isobutyl Ketone

Produkt 1

HCID 122426Bis(2-hydroxyethyl) azelate

Versuchsvorschrift

The reaction of 0.25 moles azelaic acid with 0.55 moles ethylene oxide under pressure using methyl isobutyl ketone in the presence of the catalyst of Example II (0.15% by wt. of total system) at 153° C gave bis(2-hydroxyethyl)azelate in quantitative crude yield. The material was isolated as a grey-white solid melting at 46°-47° C from a n-butyl chloride-acetone mixture in 88.5% yield.

Aufarbeitung

  1. customat 153° C

Quellen und Nachweise

ORD-Eintrag
ord-d48dd62d737a4192a0aaa9197f7a2d56
Quelldatensatz
uspto-grants-1977_04
Patentnummer
US04017429

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